Treatment of cancer cells with vitamin D3 induced death <i>a.</i> by Vidya G. Bettada (22208808)

Expression of Caspase-3 in HCT 116 and Hep 3B: <i>2A. and 2B.</i> by Vidya G. Bettada (22208808)

Number of visits per clinic type, 2013-2015. by Jacob Dreiher (14856863)

“…During PE, statistically significant longer waiting times were found for surgery (+1.0 day) and imaging (+1.1 days), while a 2.4 days decrease was noted in pediatrics, controlled for age, sex, ethnicity and the daily number of visits. …”

Treatment with vitamin D3 reduced the viability of cancer cell lines: <i>1A & 1B.</i> by Vidya G. Bettada (22208808)

“…Human and rat glioblastoma cell lines U-87 MG and C6, respectively; which were exposed to vitamin D3 demonstrated a statistically significant reduction in viable cells with increasing time and treatment concentration. 1H. …”

Vitamin D3, but not the Cisplatin, could moderately reduce STZ-induced hyperglycemia in mice (a) Schematic representation of experimental protocol followed in the study: After accl... by Vidya G. Bettada (22208808)

“…The data showed a significant increase in fasting blood glucose (FBG) beginning from day 6. …”

Comparison with Existing Studies. by Na Zhao (112953)

“…The results indicate that: (1) the presence of pores prolongs both the time to failure and the onset of the AE burst stage, with longer durations observed at higher pore dip angles; (2) AE signal amplitude and frequency vary significantly across different loading stages, and the b-value exhibits an “increase–fluctuation–decrease” trend, with the decreasing stage serving as a precursor to rock instability; (3) pore dip angle strongly influences crack propagation types: dip angles of 0°–30° favor axial cracks and through-going wing cracks, 45°–75° angles tend to induce co-planar and wing crack connectivity, while 90° angles cause crack deviation, hindering through-going failure; (4) intact rock fails in a tensile–shear mixed mode, whereas the number of shear cracks in rocks with pores initially increases and then decreases with dip angle, reaching a maximum at 45°, resulting in shear-dominated failure. …”

Specimen Preparation and Experimental Setup. by Na Zhao (112953)

“…The results indicate that: (1) the presence of pores prolongs both the time to failure and the onset of the AE burst stage, with longer durations observed at higher pore dip angles; (2) AE signal amplitude and frequency vary significantly across different loading stages, and the b-value exhibits an “increase–fluctuation–decrease” trend, with the decreasing stage serving as a precursor to rock instability; (3) pore dip angle strongly influences crack propagation types: dip angles of 0°–30° favor axial cracks and through-going wing cracks, 45°–75° angles tend to induce co-planar and wing crack connectivity, while 90° angles cause crack deviation, hindering through-going failure; (4) intact rock fails in a tensile–shear mixed mode, whereas the number of shear cracks in rocks with pores initially increases and then decreases with dip angle, reaching a maximum at 45°, resulting in shear-dominated failure. …”

UCS texts data. by Na Zhao (112953)

“…The results indicate that: (1) the presence of pores prolongs both the time to failure and the onset of the AE burst stage, with longer durations observed at higher pore dip angles; (2) AE signal amplitude and frequency vary significantly across different loading stages, and the b-value exhibits an “increase–fluctuation–decrease” trend, with the decreasing stage serving as a precursor to rock instability; (3) pore dip angle strongly influences crack propagation types: dip angles of 0°–30° favor axial cracks and through-going wing cracks, 45°–75° angles tend to induce co-planar and wing crack connectivity, while 90° angles cause crack deviation, hindering through-going failure; (4) intact rock fails in a tensile–shear mixed mode, whereas the number of shear cracks in rocks with pores initially increases and then decreases with dip angle, reaching a maximum at 45°, resulting in shear-dominated failure. …”

Log2 fold change (FC), mean and standard deviation (SD) of each lipid specie from the normal liver (NL) and metabolic dysfunction-associated steatohepatitis (MASH) groups, and adju... by Laia Bertran (3685147)

Log2 fold change (FC), mean and standard deviation (SD) of each lipid specie from the normal liver (NL) and simple steatosis (SS) groups, and adjusted p-values. by Laia Bertran (3685147)

Log2 fold change (FC), mean and standard deviation (SD) of each lipid specie from the normal liver (NL) and metabolic dysfunction-associated steatotic liver disease (MASLD) groups,... by Laia Bertran (3685147)

Log2 fold change (FC), mean and standard deviation (SD) of each lipid specie from the simple steatosis (SS) and metabolic dysfunction-associated steatohepatitis (MASH) groups, and... by Laia Bertran (3685147)

Phenotypic characterization of NMIIC knockout (KO) mice. by Hiroki Hamaguchi (22783780)

Subjects:

Spontaneous physical activity and respiratory quotient (RQ) in WT and NMIIC KO mice. by Hiroki Hamaguchi (22783780)

Subjects:

Fiber types and muscle force in the soleus of 18-20-week-old WT and NMIIC KO mice. by Hiroki Hamaguchi (22783780)

Subjects:

Phenotypic characterization of 81-week-old NMIIC KO mice. by Hiroki Hamaguchi (22783780)

Subjects:

NMIIC expression and muscle weight in the soleus of 82-86-week-old mice. by Hiroki Hamaguchi (22783780)

Subjects:

Evaluation of mitochondrial protein expression and morphology in NMIIC KO mice. by Hiroki Hamaguchi (22783780)

Subjects:

Raw data for all figures and supporting information. by Hiroki Hamaguchi (22783780)

Subjects:

Proliferation and differentiation of myoblasts derived from satellite cells in WT and NMIIC KO mice. by Hiroki Hamaguchi (22783780)

Subjects: